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Translation elicits a growth rate‐dependent, genome‐wide, differential protein production in Bacillus subtilis
Complex regulatory programs control cell adaptation to environmental changes by setting condition‐specific proteomes. In balanced growth, bacterial protein abundances depend on the dilution rate, transcript abundances and transcript‐specific translation efficiencies. We revisited the current theory...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5683663/ https://www.ncbi.nlm.nih.gov/pubmed/27193784 http://dx.doi.org/10.15252/msb.20156608 |
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author | Borkowski, Olivier Goelzer, Anne Schaffer, Marc Calabre, Magali Mäder, Ulrike Aymerich, Stéphane Jules, Matthieu Fromion, Vincent |
author_facet | Borkowski, Olivier Goelzer, Anne Schaffer, Marc Calabre, Magali Mäder, Ulrike Aymerich, Stéphane Jules, Matthieu Fromion, Vincent |
author_sort | Borkowski, Olivier |
collection | PubMed |
description | Complex regulatory programs control cell adaptation to environmental changes by setting condition‐specific proteomes. In balanced growth, bacterial protein abundances depend on the dilution rate, transcript abundances and transcript‐specific translation efficiencies. We revisited the current theory claiming the invariance of bacterial translation efficiency. By integrating genome‐wide transcriptome datasets and datasets from a library of synthetic gfp‐reporter fusions, we demonstrated that translation efficiencies in Bacillus subtilis decreased up to fourfold from slow to fast growth. The translation initiation regions elicited a growth rate‐dependent, differential production of proteins without regulators, hence revealing a unique, hard‐coded, growth rate‐dependent mode of regulation. We combined model‐based data analyses of transcript and protein abundances genome‐wide and revealed that this global regulation is extensively used in B. subtilis. We eventually developed a knowledge‐based, three‐step translation initiation model, experimentally challenged the model predictions and proposed that a growth rate‐dependent drop in free ribosome abundance accounted for the differential protein production. |
format | Online Article Text |
id | pubmed-5683663 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56836632017-11-20 Translation elicits a growth rate‐dependent, genome‐wide, differential protein production in Bacillus subtilis Borkowski, Olivier Goelzer, Anne Schaffer, Marc Calabre, Magali Mäder, Ulrike Aymerich, Stéphane Jules, Matthieu Fromion, Vincent Mol Syst Biol Articles Complex regulatory programs control cell adaptation to environmental changes by setting condition‐specific proteomes. In balanced growth, bacterial protein abundances depend on the dilution rate, transcript abundances and transcript‐specific translation efficiencies. We revisited the current theory claiming the invariance of bacterial translation efficiency. By integrating genome‐wide transcriptome datasets and datasets from a library of synthetic gfp‐reporter fusions, we demonstrated that translation efficiencies in Bacillus subtilis decreased up to fourfold from slow to fast growth. The translation initiation regions elicited a growth rate‐dependent, differential production of proteins without regulators, hence revealing a unique, hard‐coded, growth rate‐dependent mode of regulation. We combined model‐based data analyses of transcript and protein abundances genome‐wide and revealed that this global regulation is extensively used in B. subtilis. We eventually developed a knowledge‐based, three‐step translation initiation model, experimentally challenged the model predictions and proposed that a growth rate‐dependent drop in free ribosome abundance accounted for the differential protein production. John Wiley and Sons Inc. 2016-05-18 /pmc/articles/PMC5683663/ /pubmed/27193784 http://dx.doi.org/10.15252/msb.20156608 Text en © 2016 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the Creative Commons Attribution 4.0 (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Borkowski, Olivier Goelzer, Anne Schaffer, Marc Calabre, Magali Mäder, Ulrike Aymerich, Stéphane Jules, Matthieu Fromion, Vincent Translation elicits a growth rate‐dependent, genome‐wide, differential protein production in Bacillus subtilis |
title | Translation elicits a growth rate‐dependent, genome‐wide, differential protein production in Bacillus subtilis
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title_full | Translation elicits a growth rate‐dependent, genome‐wide, differential protein production in Bacillus subtilis
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title_fullStr | Translation elicits a growth rate‐dependent, genome‐wide, differential protein production in Bacillus subtilis
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title_full_unstemmed | Translation elicits a growth rate‐dependent, genome‐wide, differential protein production in Bacillus subtilis
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title_short | Translation elicits a growth rate‐dependent, genome‐wide, differential protein production in Bacillus subtilis
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title_sort | translation elicits a growth rate‐dependent, genome‐wide, differential protein production in bacillus subtilis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5683663/ https://www.ncbi.nlm.nih.gov/pubmed/27193784 http://dx.doi.org/10.15252/msb.20156608 |
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